Senior Regulatory Medical Writer III — Hybrid, Global Trials

<p>Johnson & Johnson Innovative Medicine seeks a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas within IDAR. The role may be in Maidenhead, Leiden, Neuss, Paris, or Beerse and follows a hybrid model with three onsite days weekly. </p><p>Responsibilities include writing or coordinating regulatory documents (CSRs, IBs, protocols, summaries); leading cross-functional document planning; mentoring junior writers; and driving process improvements. </p> #J-18808-Ljbffr